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GeneBe API Showcase

This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.

API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.

Documentation & Advanced Usage

Complete API documentation:docs.genebe.net/docs/api/overview/

Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/

Python client for pandas:pypi.org/project/genebe/

Java CLI for VCF files:github.com/pstawinski/genebe-cli

All tools documented at:docs.genebe.net

API Request Examples for Variant: X-18893626-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=18893626&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "X",
      "pos": 18893626,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "NM_001440805.1",
      "consequences": [
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 33,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3567G>A",
          "hgvs_p": "p.Glu1189Glu",
          "transcript": "NM_000292.3",
          "protein_id": "NP_000283.1",
          "transcript_support_level": null,
          "aa_start": 1189,
          "aa_end": null,
          "aa_length": 1235,
          "cds_start": 3567,
          "cds_end": null,
          "cds_length": 3708,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000379942.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_000292.3"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 33,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3567G>A",
          "hgvs_p": "p.Glu1189Glu",
          "transcript": "ENST00000379942.5",
          "protein_id": "ENSP00000369274.4",
          "transcript_support_level": 1,
          "aa_start": 1189,
          "aa_end": null,
          "aa_length": 1235,
          "cds_start": 3567,
          "cds_end": null,
          "cds_length": 3708,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_000292.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000379942.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2-AS1",
          "gene_hgnc_id": 44110,
          "hgvs_c": "n.467+288C>T",
          "hgvs_p": null,
          "transcript": "ENST00000452900.5",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "pseudogene",
          "feature": "ENST00000452900.5"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 33,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3591G>A",
          "hgvs_p": "p.Glu1197Glu",
          "transcript": "NM_001440805.1",
          "protein_id": "NP_001427734.1",
          "transcript_support_level": null,
          "aa_start": 1197,
          "aa_end": null,
          "aa_length": 1243,
          "cds_start": 3591,
          "cds_end": null,
          "cds_length": 3732,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001440805.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 33,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3591G>A",
          "hgvs_p": "p.Glu1197Glu",
          "transcript": "ENST00000897868.1",
          "protein_id": "ENSP00000567927.1",
          "transcript_support_level": null,
          "aa_start": 1197,
          "aa_end": null,
          "aa_length": 1243,
          "cds_start": 3591,
          "cds_end": null,
          "cds_length": 3732,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000897868.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 33,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3552G>A",
          "hgvs_p": "p.Glu1184Glu",
          "transcript": "ENST00000954730.1",
          "protein_id": "ENSP00000624789.1",
          "transcript_support_level": null,
          "aa_start": 1184,
          "aa_end": null,
          "aa_length": 1230,
          "cds_start": 3552,
          "cds_end": null,
          "cds_length": 3693,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000954730.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 33,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3540G>A",
          "hgvs_p": "p.Glu1180Glu",
          "transcript": "ENST00000897873.1",
          "protein_id": "ENSP00000567932.1",
          "transcript_support_level": null,
          "aa_start": 1180,
          "aa_end": null,
          "aa_length": 1226,
          "cds_start": 3540,
          "cds_end": null,
          "cds_length": 3681,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000897873.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3513G>A",
          "hgvs_p": "p.Glu1171Glu",
          "transcript": "NM_001440800.1",
          "protein_id": "NP_001427729.1",
          "transcript_support_level": null,
          "aa_start": 1171,
          "aa_end": null,
          "aa_length": 1217,
          "cds_start": 3513,
          "cds_end": null,
          "cds_length": 3654,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001440800.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3513G>A",
          "hgvs_p": "p.Glu1171Glu",
          "transcript": "ENST00000897869.1",
          "protein_id": "ENSP00000567928.1",
          "transcript_support_level": null,
          "aa_start": 1171,
          "aa_end": null,
          "aa_length": 1217,
          "cds_start": 3513,
          "cds_end": null,
          "cds_length": 3654,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000897869.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3483G>A",
          "hgvs_p": "p.Glu1161Glu",
          "transcript": "NM_001440801.1",
          "protein_id": "NP_001427730.1",
          "transcript_support_level": null,
          "aa_start": 1161,
          "aa_end": null,
          "aa_length": 1207,
          "cds_start": 3483,
          "cds_end": null,
          "cds_length": 3624,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001440801.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3483G>A",
          "hgvs_p": "p.Glu1161Glu",
          "transcript": "ENST00000897867.1",
          "protein_id": "ENSP00000567926.1",
          "transcript_support_level": null,
          "aa_start": 1161,
          "aa_end": null,
          "aa_length": 1207,
          "cds_start": 3483,
          "cds_end": null,
          "cds_length": 3624,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000897867.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3477G>A",
          "hgvs_p": "p.Glu1159Glu",
          "transcript": "ENST00000954732.1",
          "protein_id": "ENSP00000624791.1",
          "transcript_support_level": null,
          "aa_start": 1159,
          "aa_end": null,
          "aa_length": 1205,
          "cds_start": 3477,
          "cds_end": null,
          "cds_length": 3618,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000954732.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3468G>A",
          "hgvs_p": "p.Glu1156Glu",
          "transcript": "NM_001440802.1",
          "protein_id": "NP_001427731.1",
          "transcript_support_level": null,
          "aa_start": 1156,
          "aa_end": null,
          "aa_length": 1202,
          "cds_start": 3468,
          "cds_end": null,
          "cds_length": 3609,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001440802.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3468G>A",
          "hgvs_p": "p.Glu1156Glu",
          "transcript": "ENST00000897870.1",
          "protein_id": "ENSP00000567929.1",
          "transcript_support_level": null,
          "aa_start": 1156,
          "aa_end": null,
          "aa_length": 1202,
          "cds_start": 3468,
          "cds_end": null,
          "cds_length": 3609,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000897870.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3468G>A",
          "hgvs_p": "p.Glu1156Glu",
          "transcript": "ENST00000934920.1",
          "protein_id": "ENSP00000604979.1",
          "transcript_support_level": null,
          "aa_start": 1156,
          "aa_end": null,
          "aa_length": 1202,
          "cds_start": 3468,
          "cds_end": null,
          "cds_length": 3609,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000934920.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3435G>A",
          "hgvs_p": "p.Glu1145Glu",
          "transcript": "ENST00000934921.1",
          "protein_id": "ENSP00000604980.1",
          "transcript_support_level": null,
          "aa_start": 1145,
          "aa_end": null,
          "aa_length": 1191,
          "cds_start": 3435,
          "cds_end": null,
          "cds_length": 3576,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000934921.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3432G>A",
          "hgvs_p": "p.Glu1144Glu",
          "transcript": "ENST00000954728.1",
          "protein_id": "ENSP00000624787.1",
          "transcript_support_level": null,
          "aa_start": 1144,
          "aa_end": null,
          "aa_length": 1190,
          "cds_start": 3432,
          "cds_end": null,
          "cds_length": 3573,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000954728.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3429G>A",
          "hgvs_p": "p.Glu1143Glu",
          "transcript": "ENST00000934923.1",
          "protein_id": "ENSP00000604982.1",
          "transcript_support_level": null,
          "aa_start": 1143,
          "aa_end": null,
          "aa_length": 1189,
          "cds_start": 3429,
          "cds_end": null,
          "cds_length": 3570,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000934923.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3414G>A",
          "hgvs_p": "p.Glu1138Glu",
          "transcript": "NM_001440803.1",
          "protein_id": "NP_001427732.1",
          "transcript_support_level": null,
          "aa_start": 1138,
          "aa_end": null,
          "aa_length": 1184,
          "cds_start": 3414,
          "cds_end": null,
          "cds_length": 3555,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001440803.1"
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHKA2",
          "gene_hgnc_id": 8926,
          "hgvs_c": "c.3414G>A",
          "hgvs_p": "p.Glu1138Glu",
          "transcript": "ENST00000954729.1",
          "protein_id": "ENSP00000624788.1",
          "transcript_support_level": null,
          "aa_start": 1138,
          "aa_end": null,
          "aa_length": 1184,
          "cds_start": 3414,
          "cds_end": null,
          "cds_length": 3555,
          "cdna_start": null,
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      "acmg_classification": "Benign",
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            "BS2"
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          "inheritance_mode": "",
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      "clinvar_disease": "Glycogen storage disease IXa1",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "Glycogen storage disease IXa1",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
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  ],
  "message": null
}